A New Power Dissipation Model and Its Analytic Formulation for Electric-Field-Driven Water Dissociation in the Cationic/Anionic Bipolar Polymer Membrane Junctions

Bipolar Polymer Membranes (BPMs) enable the creation of large, stable pH gradients by driving water dissociation (WD) at the cation/anion junction under reverse bias, a process central to electrodialysis, CO₂ capture, and emerging acid-alkaline water electrolysis. Yet despite decades of study, the mechanism by which intense interfacial electric fields accelerate WD remains debated and is often modeled with ad hoc assumptions. In this study, we present a power dissipation model in which minority ions from water autoprotolysis act as carriers that continuously dissipate field-supplied power in the hydrated nanometric junction. This dissipative input increases the local probability of heterolytic O-H bond cleavage and analytically leads to a quadratic dependence of the dissociation rate constant on the field. Without adjustable parameters, the model reproduces the required orders of magnitude for the enhancement ratio <i>k_d</i>(<i>E</i>)/<i>k_d</i>(0), where <i>k_d</i>(<i>E</i>) is the field-enhanced water dissociation rate constant and <i>k_d</i>(0) is its zero-field value across typical BPM fields, and yields a quadratic current-voltage junction law. A proof-of-principle measurement on a commercial Fumasep^® FBM bipolar membrane confirms the quadratic current-voltage trend, supporting a power-dissipation-driven water dissociation mechanism and providing a concise, falsifiable baseline for future studies.